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Opening Plenary Session
Session Chair(s)
Omprakash Sadhwani
Ex-Joint Commissioner (HQ) and Drugs Controller
Maharashtra Food and Drug Administration, India
The Regulators have been extremely diligent on implementing regulations in their respective jurisdiction in last 6 years. In particular, the medical device regulations in various parts of the world From India MDR and EU MDR in 2017 to UKCA regulations by MHRA and latest changes to the China, Australia regulations Medical Device Regulations regulatory developments. The Clinical Research regulations are another set of dynamic regulations, which are in constant evolution. In this session, let’s hear from the Masters about regulations and their vision.
Speaker(s)
India Regulatory Environment For Medical Products And Clinical Research
Representative Invited
Central Drugs Standard Control Organization, India
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